Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17257269
rs17257269
FHIT
1.000 0.080 3 60039779 intron variant T/C snv 0.15
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs9874888
rs9874888
FHIT
1.000 0.080 3 60030591 intron variant T/A snv 0.30
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009